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Nature Chemical Biology
|
June 11, 2019
BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design
William Farnaby, Manfred Koegl, Michael J Roy, et al.
Nature Chemical Biology
|
July 4, 2019
Publisher Correction: BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design
William Farnaby, Manfred Koegl, Michael J Roy, et al.
Journal of Medicinal Chemistry
|
August 1, 2019
Intracellular Trapping of the Selective Phosphoglycerate Dehydrogenase (PHGDH) Inhibitor <b>BI-4924</b> Disrupts Serine Biosynthesis
Harald Weinstabl, Matthias Treu, Joerg Rinnenthal, et al.
Nature Cancer
|
August 5, 2024
Co-targeting SOS1 enhances the antitumor effects of KRAS<sup>G12C</sup> inhibitors by addressing intrinsic and acquired resistance
Venu Thatikonda, Hengyu Lyu, Sabine Jurado, et al.
Nature Cancer
|
July 26, 2022
Discovery of potent and selective HER2 inhibitors with efficacy against HER2 exon 20 insertion-driven tumors, which preserve wild-type EGFR signaling
Birgit Wilding, Dirk Scharn, Dietrich Böse, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 24, 2019
Drugging an undruggable pocket on KRAS
Dirk Kessler, Michael Gmachl, Andreas Mantoulidis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 13, 2020
Reply to Tran et al.: Dimeric KRAS protein-protein interaction stabilizers
Dirk Kessler, Andreas Gollner, Michael Gmachl, et al.
Cell Reports
|
September 21, 2017
Chemically Induced Degradation of the Oncogenic Transcription Factor BCL6
Nina Kerres, Steffen Steurer, Stefanie Schlager, et al.
Nature Chemical Biology
|
July 10, 2019
Fragment-based discovery of a chemical probe for the PWWP1 domain of NSD3
Jark Böttcher, David Dilworth, Ulrich Reiser, et al.
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Search research articles
Search
Showing results (161-170 of 169) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 169 results.
Nature Chemical Biology
|
June 11, 2019
BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design
William Farnaby, Manfred Koegl, Michael J Roy, et al.
Nature Chemical Biology
|
July 4, 2019
Publisher Correction: BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design
William Farnaby, Manfred Koegl, Michael J Roy, et al.
Journal of Medicinal Chemistry
|
August 1, 2019
Intracellular Trapping of the Selective Phosphoglycerate Dehydrogenase (PHGDH) Inhibitor <b>BI-4924</b> Disrupts Serine Biosynthesis
Harald Weinstabl, Matthias Treu, Joerg Rinnenthal, et al.
Nature Cancer
|
August 5, 2024
Co-targeting SOS1 enhances the antitumor effects of KRAS<sup>G12C</sup> inhibitors by addressing intrinsic and acquired resistance
Venu Thatikonda, Hengyu Lyu, Sabine Jurado, et al.
Nature Cancer
|
July 26, 2022
Discovery of potent and selective HER2 inhibitors with efficacy against HER2 exon 20 insertion-driven tumors, which preserve wild-type EGFR signaling
Birgit Wilding, Dirk Scharn, Dietrich Böse, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 24, 2019
Drugging an undruggable pocket on KRAS
Dirk Kessler, Michael Gmachl, Andreas Mantoulidis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 13, 2020
Reply to Tran et al.: Dimeric KRAS protein-protein interaction stabilizers
Dirk Kessler, Andreas Gollner, Michael Gmachl, et al.
Cell Reports
|
September 21, 2017
Chemically Induced Degradation of the Oncogenic Transcription Factor BCL6
Nina Kerres, Steffen Steurer, Stefanie Schlager, et al.
Nature Chemical Biology
|
July 10, 2019
Fragment-based discovery of a chemical probe for the PWWP1 domain of NSD3
Jark Böttcher, David Dilworth, Ulrich Reiser, et al.
Page
of 17